Ma. Nosek et Ca. Howland, PERSONAL ASSISTANCE SERVICES - THE HUB OF THE POLICY WHEEL FOR COMMUNITY INTEGRATION OF PEOPLE WITH SEVERE PHYSICAL-DISABILITIES, Policy studies journal, 21(4), 1993, pp. 789-800
The success of persons with severe physical disabilities in living ind
ependently in the community, engaging in self-directed productive acti
vities, and staying healthy depends, in part, on getting and maintaini
ng adequate personal assistance with basic tasks such as getting out o
f bed and tending to personal hygiene. Although few policymakers would
disagree with the contention thal many people with disabilities need
assistance with daily tasks, there is considerable debate about who sh
ould provide assistance, what services should be included, who should
pay, who should be entitled to publicly provided and paid services, ho
w much assistance should be provided, and who should control its admin
istration. The prevailing model for delivery of personal assistance se
rvices has been primarily medical, with control of services by health
care professionals, rather than independent living, with control by co
nsumers receiving services. Traditionally there has been an institutio
nal bias of funding for disability-related service, despite its much h
igher expense than community-based personal assistance services and it
s violation of basic human rights. Proponents of various solutions to
health care reform have given little consideration to the provision of
support services for people with disabilities. The advantages of impl
ementing a uniform national system for the delivery of personal assist
ance services based on consumer control are discussed.